4.8 Article

Topotactic Transformation of Surface Structure Enabling Direct Regeneration of Spent Lithium-Ion Battery Cathodes

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 145, Issue 13, Pages 7288-7300

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.2c13151

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Recycling spent lithium-ion batteries (LIBs) is crucial to address resource shortage and environmental pollution. A challenge in direct recycling of spent LiNi0.5Co0.2Mn0.3O2 (NCM523) cathode is the disruption of Li+ transport due to electrostatic repulsion from a rock salt/spinel phase formed on the cycled cathode surface. In this study, a topotactic transformation of the rock salt/spinel phase into Ni0.5Co0.2Mn0.3(OH)2 and then back to NCM523 cathode was proposed, enabling improved lithium replenishment and comparable performance to pristine cathodes after regeneration.
Recycling spent lithium-ion batteries (LIBs) has become an urgent task to address the issues of resource shortage and potential environmental pollution. However, direct recycling of the spent LiNi0.5Co0.2Mn0.3O2 (NCM523) cathode is challenging because the strong electrostatic repulsion from a transition metal octahedron in the lithium layer provided by the rock salt/spinel phase that is formed on the surface of the cycled cathode severely disrupts Li+ transport, which restrains lithium replenishment during regeneration, resulting in the regenerated cathode with inferior capacity and cycling performance. Here, we propose the topotactic transformation of the stable rock salt/spinel phase into Ni0.5Co0.2Mn0.3(OH)2 and then back to the NCM523 cathode. As a result, a topotactic relithiation reaction with low migration barriers occurs with facile Li+ transport in a channel (from one octahedral site to another, passing through a tetrahedral intermediate) with weakened electrostatic repulsion, which greatly improves lithium replenishment during regeneration. In addition, the proposed method can be extended to repair spent NCM523 black mass, spent LiNi0.6Co0.2Mn0.2O2, and spent LiCoO2 cathodes, whose electrochemical performance after regeneration is comparable to that of the commercial pristine cathodes. This work demonstrates a fast topotactic relithiation process during regeneration by modifying Li+ transport channels, providing a unique perspective on the regeneration of spent LIB cathodes.

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